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Thomas Meitinger

Showing results (11-20 of 536) with videos related to

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IEEE/ACM Transactions on Computational Biology and Bioinformatics|October 20, 2006
Gene mapping and marker clustering using Shannon's mutual informationZaher Dawy, Bernhard Goebel, Joachim Hagenauer, et al.
Annals of Clinical and Translational Neurology|February 28, 2020
Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorderTheresa Brunet, Milena Radivojkov-Blagojevic, Peter Lichtner, et al.
Journal of Molecular and Cellular Cardiology|August 2, 2016
Characterization of circular RNAs in human, mouse and rat heartsStanislas Werfel, Stephan Nothjunge, Thomas Schwarzmayr, et al.
Ebiomedicine|February 18, 2022
Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databasesHana Kolarova, Jing Tan, Tim M Strom, et al.
International Journal of Cardiology|January 22, 2017
Genome-wide association study in takotsubo syndrome - Preliminary results and future directionsIngo Eitel, Christian Moeller, Matthias Munz, et al.
Stroke|March 8, 2008
Genetic variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populationsSteve Bevan, Martin Dichgans, H Erich Wiechmann, et al.
Molecular Biotechnology|September 10, 2008
MitoP2: an integrative tool for the analysis of the mitochondrial proteomeMatthias Elstner, Christophe Andreoli, Uwe Ahting, et al.
Gene|March 25, 2017
Identification of a de novo microdeletion 1q44 in a patient with hypogenesis of the corpus callosum, seizures and microcephaly - A case reportDominik S Westphal, Stephanie Andres, Kirsten I Beitzel, et al.
Neurology. Genetics|August 13, 2019
Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencingMartin Krenn, Ivan Milenkovic, Gertrud Eckstein, et al.
Plos Genetics|October 25, 2011
A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrierAnne Wöhlke, Ute Philipp, Patricia Bock, et al.
Pageof 54

Showing results (11-20 of 536) with videos related to

Sort By:
Pageof 54
IEEE/ACM Transactions on Computational Biology and Bioinformatics|October 20, 2006
Gene mapping and marker clustering using Shannon's mutual informationZaher Dawy, Bernhard Goebel, Joachim Hagenauer, et al.
Annals of Clinical and Translational Neurology|February 28, 2020
Biallelic loss-of-function variants in RBL2 in siblings with a neurodevelopmental disorderTheresa Brunet, Milena Radivojkov-Blagojevic, Peter Lichtner, et al.
Journal of Molecular and Cellular Cardiology|August 2, 2016
Characterization of circular RNAs in human, mouse and rat heartsStanislas Werfel, Stephan Nothjunge, Thomas Schwarzmayr, et al.
Ebiomedicine|February 18, 2022
Lifetime risk of autosomal recessive neurodegeneration with brain iron accumulation (NBIA) disorders calculated from genetic databasesHana Kolarova, Jing Tan, Tim M Strom, et al.
International Journal of Cardiology|January 22, 2017
Genome-wide association study in takotsubo syndrome - Preliminary results and future directionsIngo Eitel, Christian Moeller, Matthias Munz, et al.
Stroke|March 8, 2008
Genetic variation in members of the leukotriene biosynthesis pathway confer an increased risk of ischemic stroke: a replication study in two independent populationsSteve Bevan, Martin Dichgans, H Erich Wiechmann, et al.
Molecular Biotechnology|September 10, 2008
MitoP2: an integrative tool for the analysis of the mitochondrial proteomeMatthias Elstner, Christophe Andreoli, Uwe Ahting, et al.
Gene|March 25, 2017
Identification of a de novo microdeletion 1q44 in a patient with hypogenesis of the corpus callosum, seizures and microcephaly - A case reportDominik S Westphal, Stephanie Andres, Kirsten I Beitzel, et al.
Neurology. Genetics|August 13, 2019
Adult-onset variant ataxia-telangiectasia diagnosed by exome and cDNA sequencingMartin Krenn, Ivan Milenkovic, Gertrud Eckstein, et al.
Plos Genetics|October 25, 2011
A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrierAnne Wöhlke, Ute Philipp, Patricia Bock, et al.
Pageof 54